Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6478317 0.882 0.120 9 117701903 upstream gene variant G/A snv 3
rs11719165 0.925 0.040 3 194865359 intergenic variant T/C snv 0.53 2
rs117829974 1.000 0.040 3 62886233 intergenic variant C/A;G;T snv 2
rs12046844 0.925 0.040 1 65772696 regulatory region variant G/A snv 0.17 2
rs1901440 0.925 0.040 2 133680388 intergenic variant C/A snv 0.58 2
rs2501846 1.000 0.040 1 212668592 upstream gene variant T/C snv 0.24 2
rs7091672 0.925 0.040 10 118836909 intron variant T/A;C;G snv 2
rs16957920 1.000 0.040 13 87710848 intergenic variant G/C snv 6.4E-02 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs12720066
ABCB1
0.925 0.040 7 87540386 intron variant A/C snv 3.9E-02 2
rs200754866
ABCB1
1.000 0.040 7 87536484 missense variant C/A;T snv 1.2E-05; 3.6E-05 1
rs966923314
ABCB1
1.000 0.040 7 87601026 5 prime UTR variant T/C snv 7.0E-06 1
rs2074087
ABCC1
0.882 0.080 16 16090375 intron variant C/G snv 0.81 0.83 3
rs1260186456
ABCC1
0.925 0.040 16 16102659 missense variant G/T snv 9.4E-06 2
rs17501331
ABCC1
0.925 0.040 16 15995584 intron variant A/G snv 7.7E-02 2
rs17822471
ABCC11
1.000 0.040 16 48208468 missense variant G/A snv 5.1E-02 4.8E-02 1
rs3740066
ABCC2
0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs717620
ABCC2
0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs1885301
ABCC2
0.925 0.040 10 99781296 upstream gene variant A/G snv 0.58 2
rs4148396
ABCC2
0.925 0.040 10 99832187 intron variant T/C snv 0.65 2
rs3765534
ABCC4
0.882 0.200 13 95163161 missense variant C/T snv 2.3E-02 1.2E-02 4
rs9561778
ABCC4
0.851 0.120 13 95061461 intron variant G/A;T snv 4
rs763794263
ABCC8
1.000 0.040 11 17432232 missense variant G/A snv 6.3E-05 3.5E-05 1